A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5917473



Internal ID22692692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62209635..62237812hg38UCSC Ensembl
chr11:61977107..62005284hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3828178
hg1928178
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17353112
Samples
Known GenesSCGB2A1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5917473
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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